Impact of EU MDR on Notified Bodies

Impact of EU MDR on Notified Bodies Examining the Effects of EU MDR Implementation As medical device companies are beginning to transition towards the EU Medical Device Regulation standards, there is no denying that Notified Bodies are also making strides to meet the...
Understanding the FDA Cybersecurity Go-Team

Understanding the FDA Cybersecurity Go-Team

Understanding the FDA Cybersecurity Go-Team The U.S. Food and Drug Administration (FDA) recently unveiled the Medical Device Safety Action Plan: Protecting Patients, Promoting Public Health, a comprehensive plan with the goal of assessing processes and procedures in...
From On-Screen To Real Life

From On-Screen To Real Life

From On-Screen To Real Life "Chicago Med" Explores FDA Guidelines The US Food and Drug Administration (FDA) recently released a new medical device safety action plan that contains five focus areas that aim to improve the quality of real-world evidence,...

5 Things to Consider When Choosing a Supplier

Top Five Things to Consider When Choosing your Supplier We Asked Industry Experts. Here’s What We Found. As medical devices become increasingly complex, the need for reliable, compliant, and cost-efficient supplier partners is of great importance to strategic sourcing...